The US Food and Drug Administration (USFDA) has completed evaluation of Divis Laboratories corrective actions in response to its Warning Letter dated April 13, 2017. The agency has closed-out the warning letter.
Divis Laboratories focussed on developing new processes for the production of Active Pharma Ingredients (APIs) & Intermediates. The company in a matter of short time expanded its breadth of operations to provide complete turnkey solutions to the domestic Indian pharmaceutical industry.